Total Syntheses of (−)-Methyl Atis-16-en-19-oate, (−)-Methyl Kaur-16-en-19-oate, and (−)-Methyl Trachyloban-19-oate by a Combination of Palladium-Catalyzed Cycloalkenylation and Homoallyl−Homoallyl Radical Rearrangement-Reference-Cited by-同舟云学术

Total Syntheses of (−)-Methyl Atis-16-en-19-oate, (−)-Methyl Kaur-16-en-19-oate, and (−)-Methyl Trachyloban-19-oate by a Combination of Palladium-Catalyzed Cycloalkenylation and Homoallyl−Homoallyl Radical Rearrangement

Published:2000-06-28 Issue:15 Volume:65 Page:4565-4570
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Toyota Masahiro¹,Wada Toshihiro¹,Ihara Masataka¹

Affiliation:

1. Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo000142b

Reference14 articles.

1. A Formal Total Synthesis of (+)-Methyl Trachyloban-18-oate and (+)-Methyl 16-Oxo-17-norkauran-18-oate: Regio- and Diastereoselective Preparation of Methyl (13S)-13-Hydroxyisoatisiren-18-oate from (?)-Abietic Acid

2. Total Synthesis of (±)-Methyl Atis-16-en-19-oate via Homoallyl−Homoallyl Radical Rearrangement

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